Law Updates

Subject

Summary: The Bureau of Indian Standards ( BIS ) has amended three Indian Standards covering shuttering plywood, hearing protectors and stainless steel sinks for domestic use. The affected standards are IS 4990:2024, IS 9167:2025 and IS 13983:1994. The amendments were established on 3 August 2026. The notification is dated 5 August 2026, and was published in the Gazette of India on 12 August 2026 under reference HQ-PUB015/1/2020-PUB-BIS (1585). The earlier versions of the three standards will continue to apply until 2 February 2027. This transition period is important for manufacturers, licence holders, testing teams, buyers, and suppliers dealing with these products. They should review the amendments and check whether the changes affect their product specifications, testing, quality checks or related documents. The notice establishes the amendments and the concurrent-validity dates. It does not reproduce the amended clauses or introduce a standalone certification process, fee, testing method or penalty. Notification at a Glance Particular Verified Details Issuing authority Bureau of Indian Standards, Department of Consumer Affairs Document type BIS notification establishing amendments to Indian Standards Reference number HQ-PUB015/1/2020-PUB-BIS (1585) Notification date 5 August 2026 Gazette publication date 12 August 2026 Date of establishment of amendments 3 August 2026 Governing provision Rule 15(1) of the Bureau of Indian Standards Rules, 2018 Standards covered IS 4990:2024, IS 9167:2025 and IS 13983:1994 Main stakeholders IS 4990:2024, IS 9167:2025 and IS 13983:1994 Core development BIS established one amendment for each of IS 4990 and IS 9167, and Amendment No. 4 for IS 13983 Transition end date 2 February 2027 Effective date The amendments were established on 3 August 2026; a separate commencement date is not expressly specified Nature of requirement Standards notification; the detailed technical changes are not reproduced in the Gazette notice The dates have different functions. The amendments were established on 3 August, the notification bears the date 5 August and the Gazette was published on 12 August 2026. The unamended standards may remain in force only up to 2 February 2027, as stated in the schedule. The Regulatory Framework BIS issued the notification under Rule 15(1) of the Bureau of Indian Standards Rules, 2018. Rule 15 deals with the establishment, review, revision and amendment of Indian Standards. It provides the mechanism through which BIS may establish an amendment and notify the period for which an existing standard may continue alongside the amended position. This notification performs that standards-management function. It identifies the affected Indian Standards, the number and month of each amendment, the date on which each amendment was established and the date until which the standard without that amendment may remain in force. An Indian Standard notification should not automatically be treated as a new Quality Control Order or a fresh certification mandate. Whether a product must carry the Standard Mark or operate under BIS certification depends on the applicable governing law, Quality Control Order, certification scheme and other official directions. Those questions must be assessed separately for each product and business. Scope and Applicability The notification applies only to the three standards specifically mentioned in it and the amendments made to those standards. It should not be read as a wider change covering all types of plywood, hearing protection products, or stainless steel products. Businesses should check whether their particular product falls under any of the three standards before making changes to their compliance process. Product or Standard Covered by This Notice? Relevant Condition Main Review Area Plywood for concrete shuttering works under IS 4990:2024 Yes Amendment No. 1, August 2026 Technical specification, product testing, declarations and marking should be checked against the amendment text Hearing protectors under IS 9167:2025 Yes Amendment No. 1, August 2026 Product and test requirements should be checked against the amendment text Stainless steel sinks for domestic purposes under IS 13983:1994 Yes Amendment No. 4, August 2026 Material, construction, performance and marking provisions should be checked against the amendment text Products outside these three standards No direct coverage stated No amendment is announced for them in this notice Check their own applicable standards and regulatory instruments The notice does not list exemptions, business-size relaxations or separate dates for domestic manufacturers, foreign manufacturers, importers or micro, small and medium enterprises (MSMEs). What Has Changed BIS has established one identified amendment for each of the three standards. The Gazette does not show the clause-level changes, so the precise earlier and new technical positions cannot be compared from this notice alone. Compliance Area Earlier Position New Position Relevant Date Business Meaning IS 4990:2024 Standard operated without Amendment No. 1 Amendment No. 1, August 2026, has been established 3 August 2026 Obtain the amendment and review its effect on applicable plywood specifications and compliance evidence IS 9167:2025 Standard operated without Amendment No. 1 Amendment No. 1, August 2026, has been established 3 August 2026 Review the amendment before making technical, testing or product-control changes IS 13983:1994 Standard included amendments preceding Amendment No. 4 Amendment No. 4, August 2026, has been established 3 August 2026 Review the amendment before making technical, testing or product-control changes Concurrent validity Unamended versions continued to apply Standards without the listed amendments may remain in force until 2 February 2027 Up to 2 February 2027 Plan implementation within the stated transition window The notification establishes a common transition date for all three standards. It does not state that every affected business must complete an identical process, because the necessary action will depend on the amendment text and the entity's certification or commercial position. Product-Wise Analysis of the BIS Amendments 2026 IS 4990:2024 - Plywood for Concrete Shuttering Works BIS has established Amendment No. 1 of August 2026 to IS 4990:2024, Plywood for Concrete Shuttering Works - Specification (Fourth Revision). The amendment was established on 3 August 2026. IS 4990:2024 without Amendment No. 1 may remain in force until 2 February 2027. BIS material describing IS 4990:2024 states that the standard covers plywood used for shuttering and formwork in construction. It identifies plain, polymer-coated and film-faced types, as well as E1 and E2 formaldehyde classifications. The standard addresses matters such as raw materials, dimensions, workmanship, water resistance, strength, preservative retention and formaldehyde-related testing. That background explains why a technical review may affect product manuals, test facilities, test reports, specifications, declarations or marking. However, the August 2026 Gazette notice does not say which of those areas Amendment No. 1 changes. Businesses should not reuse the change list from the original 2024 revision as though it describes the 2026 amendment. IS 9167:2025 - Hearing Protectors BIS has established Amendment No. 1 of August 2026 to IS 9167:2025, Hearing Protectors - Specification (First Revision). The date of establishment is 3 August 2026, while the standard without the amendment may remain in force until 2 February 2027. The product title indicates that the standard concerns hearing protectors. The notification does not identify particular device types, performance values, attenuation requirements, test methods, markings or user-information changes. Manufacturers and laboratories therefore need the official Amendment No. 1 text before modifying product specifications or testing programmes. The notice also does not state that the amendment creates a new legal duty to obtain BIS certification. Any certification or market-access conclusion must be based on the separate legal instrument applicable to the product. IS 13983:1994 - Stainless Steel Sinks for Domestic Purposes BIS has established Amendment No. 4 of August 2026 to IS 13983:1994, Stainless Steel Sinks for Domestic Purposes - Specification. The amendment was established on 3 August 2026. The standard without Amendment No. 4 may remain in force until 2 February 2027. The standard is confined by its title to stainless steel sinks intended for domestic purposes. The Gazette notice does not extend the amendment to all stainless steel products or every type of commercial sink. It also does not reproduce changes concerning steel grade, thickness, dimensions, workmanship, corrosion performance, fitting features, marking or tests. BIS has earlier listed IS 13983:1994 in its consumer information on mandatory certification for certain cookware, utensils, and cans. However, businesses should refer to the current Quality Control Order, and relevant BIS certification requirements to confirm whether certification applies. The August 2026 standards notification itself should not be treated as the basis for that requirement. Implementation Timeline and Concurrent Validity All three amendments follow the same schedule. Event Date Affected Stakeholders Practical Action Amendments established by BIS 3 August 2026 Businesses and technical teams using the three standards Obtain the amendment texts and begin impact assessment BIS notification dated 5 August 2026 Regulatory, legal and compliance teams Record the official reference and scope Gazette publication 12 August 2026 All relevant stakeholders Treat the notice as officially published and plan within the transition window Last date on which the standards without the listed amendments may remain in force 2 February 2027 Users of the unamended standards Complete the applicable technical and documentary transition before the old position ceases to remain in force The Gazette does not call 2 February 2027 a general licence-renewal or certification deadline. It is the date until which each standard without the specified amendment may remain in force. The effect on an individual licence, pending application, product test report or production batch must be confirmed under the applicable BIS implementation directions. Information Not Expressly Specified The short Gazette notification does not provide the substantive contents of the three amendments. It also does not expressly specify: The clauses, tables, annexures or test methods changed by each amendment Revised technical values, tolerances, performance criteria or sampling plans Product-marking, packaging or labelling changes A separate date on which each new technical clause becomes compulsory, apart from the establishment and concurrent-validity dates stated Procedures for existing BIS licence holders or pending applicants Retesting, factory inspection, surveillance or audit requirements Forms, declarations, reports or records to be submitted Fees, deposits or other financial amounts Exemptions or special treatment for MSMEs, startups, importers or foreign manufacturers Penalties or enforcement consequences Treatment of stock manufactured, imported, contracted or tested before the transition ends These omissions do not mean that no connected requirements exist. They mean those requirements cannot be derived from this notification and must be checked in the actual amendments, applicable certification scheme, Quality Control Order, product manual and implementation guidelines. Separate Documents Businesses Must Consult Implementation requires more than the two-page Gazette notice. Document Status in the Supplied Source Why It Is Needed Amendment No. 1, August 2026, to IS 4990:2024 Identified but not reproduced Reveals the clause-level technical change for shuttering plywood Amendment No. 1, August 2026, to IS 9167:2025 Identified but not reproduced Reveals the revised requirements for hearing protectors Amendment No. 4, August 2026, to IS 13983:1994 Identified but not reproduced Reveals the revised requirements for domestic stainless steel sinks Current product manual and scheme of inspection and testing, where applicable Not identified in the Gazette May govern testing, marking and licence controls Product-specific BIS implementation guidelines Not identified in the Gazette May explain transition treatment for licensees and applicants Current Quality Control Order or other mandatory instrument, where applicable Not identified in the Gazette Determines whether compliance or certification is legally compulsory for a given product and entity Only current official versions should be used. Internal specifications and supplier contracts may then be checked against the verified legal and technical position. Impact on Businesses The immediate effect is a need for targeted review rather than an assumption that every process has changed. The level of work will depend on the actual amendment and the stakeholder's role. Manufacturers and Existing Licence Holders Manufacturers using any of the three standards should identify affected products and obtain the amendment text. Existing licence holders may need to compare their product design, raw materials, manufacturing controls, test facilities, marking, declarations and records with the amended clauses. Any licence-specific action should follow official BIS directions rather than a generic process. Applicants and Product-Development Teams Pending applicants and businesses developing products against these standards should confirm which version BIS will accept at each stage. Technical files, drawings, bills of material, inspection plans, and laboratory instructions may need revision if the amendment changes a relevant clause. Laboratories and Quality Teams Do not change a testing method just because a new amendment has been issued. First check the actual changes in the standard. There may be changes to equipment, samples, test conditions, calculations, acceptance limits, or test reports. Keep a clear record of which version was followed. Importers, Buyers and Supply Chain Partners There is no direct requirement for importers, distributors, or buyers in this notification. However, they should check the standard version mentioned in product documents, certificates, test reports and purchase orders. For orders that will continue after the transition period, the technical details may need to be reviewed and updated. Stakeholder Immediate Impact Likely Operational Effect Priority Concern Manufacturer Amendment impact review Possible updates to product controls and technical evidence Obtain official amendment text Existing licence holder Check BIS transition directions Possible licence-scope or evidence update Confirm action with the relevant BIS office or official guideline Applicant Verify acceptable standard version Possible change to application or test evidence Avoid relying on an obsolete version after transition Laboratory Review technical changes Possible method, equipment or report update Do not infer tests from the notice alone Buyer or importer Review specifications and supplier evidence Contract and procurement updates may be needed Align orders scheduled after 2 February 2027 Risks and Practical Considerations No fine, prosecution, cancellation, recall or seizure is stated in this notification. It would therefore be inaccurate to assign a statutory penalty to the notice itself. The risks mainly arise when businesses fail to address the changes within the required period. These may include reliance on an outdated technical reference, incomplete test records, differences in supplier specifications, delayed updates or product documents that do not match the revised standard. Where a separate mandatory certification requirement applies, failure to follow the revised requirements may also affect the certification process. The exact impact will depend on the applicable certification scheme, and should be confirmed from the relevant BIS requirements. Businesses should also avoid assuming that the same action applies to all three products. Each amendment may address different technical subjects. What Businesses Should Do Next Confirm product coverage. Map products and models against the exact titles and numbers of IS 4990:2024, IS 9167:2025 and IS 13983:1994. Obtain the official amendments. Secure the three August 2026 amendment texts from BIS. Do not rely on the Gazette schedule as a substitute for their technical content. Compare affected clauses. Create a controlled comparison of the current requirement, amended requirement, evidence of conformity and responsible department. Check certification status separately. Determine whether a current Quality Control Order, BIS certification scheme, product manual or licence condition applies to the specific product and business. Review implementation directions. Look for product-specific BIS guidelines covering existing licences, applications, testing, endorsements, surveillance or scope changes. Update internal and commercial documents. Where the amendment requires it, revise specifications, drawings, inspection plans, test instructions, supplier requirements, purchase orders, labels and records. Plan ahead of 2 February 2027. Use the transition period to review the changes and complete any required updates before the older standards are withdrawn. Keep clear records of the standard and amendment version followed. Seek clarification when needed. If any technical or licensing requirement is unclear, check with BIS or a qualified professional. Do not make compliance decisions based on assumptions. How Corpseed Can Help? Corpseed can support manufacturers, applicants, importers and other affected businesses in converting the notification into a product-specific action plan. A BIS certification consultant can help distinguish the amendment notice from separate mandatory certification requirements and identify the official documents that control implementation. Relevant support may include: Product and standard applicability assessment Retrieval and review of applicable BIS amendments and official directions Clause-level compliance gap assessment Review of current Quality Control Orders and certification status BIS application and licence-support documentation, where required Technical-file, test-report and product-manual review Coordination support for recognised laboratory testing, where applicable Transition planning for existing licences and pending applications Corpseed's role is to organise the applicable requirements, documentation and stakeholder actions. Certification, approval and timelines remain subject to the governing rules, technical conformity and decisions of the competent authority. Businesses dealing with shuttering plywood, hearing protectors or domestic stainless steel sinks may contact Corpseed for document-specific BIS certification services and technical compliance consulting before the 2 February 2027 transition date. Key Takeaways The BIS 2026 notification updates three Indian Standards and gives businesses time to move from the older versions to the amended ones. However, the notification does not explain the changes in detail. Businesses should read the official amendment documents, and check any product-specific requirements before making changes to their testing, product specifications, or certification processes. Amendment No. 1 applies to IS 4990:2024 for plywood used in concrete shuttering works. Amendment No. 1 applies to IS 9167:2025 for hearing protectors. Amendment No. 4 applies to IS 13983:1994 for domestic stainless steel sinks. All three amendments were established on 3 August 2026. The standards without the listed amendments may remain in force until 2 February 2027. The notice does not state technical changes, fees, procedures, exemptions or penalties. Product-specific certification and implementation duties must be verified separately.

Subject

Summary: The BIS Indian Standards notification 2026 has established nine standards through Ref. HQ-PUB013/1/2020-PUB-BIS (1583), dated 5 August 2026 and published in the Gazette of India on 12 August 2026. All nine standards have an establishment date of 3 August 2026. They cover industrial chemicals, chemical-safety codes, animal-feed material, homoeopathic preparations, traditional medicine and the safe handling of biotherapeutic products. Four are revised standards. Their earlier versions remain in force concurrently until 3 February 2027 and are scheduled to be withdrawn on that date. The remaining five entries have no earlier standard identified in the notification. Manufacturers, laboratories, procurement teams, product developers, safety professionals and businesses using these standards should review the correct 2026 edition. The notification establishes and transitions standards, it does not, by itself, state that BIS certification , registration, testing or licensing is mandatory for the listed products. Notification at a Glance Particular Verified details Issuing authority Bureau of Indian Standards, Department of Consumer Affairs Document type Gazette notification establishing and revising Indian Standards Reference number HQ-PUB013/1/2020-PUB-BIS (1583) Gazette identifier CG-DL-E-12082026-275420, Gazette No. 497 Notification date 5 August 2026 Gazette publication date 12 August 2026 Date of establishment 3 August 2026 for all nine standards Separate effective date Not expressly specified, the schedule gives 3 August 2026 as the establishment date Governing provision cited Rule 15(1) of the Bureau of Indian Standards Rules, 2018 Sectors covered Industrial chemicals, chemical safety, animal feed, homoeopathy and traditional medicine Main stakeholders Manufacturers, users, laboratories, procurement and quality teams, product developers and standard users Core development Nine standards established: four revisions and five entries with no predecessor listed Transition deadline 3 February 2027 for withdrawal of the four identified older standards Nature of requirement Establishment, revision, concurrent running and scheduled withdrawal of standards, no certification mandate is stated in this notification The date sequence matters. The standards were established on 3 August, the notification is dated 5 August, and the Gazette published it on 12 August 2026. Businesses should not describe the publication date as the establishment date. The Regulatory Framework The Bureau of Indian Standards (BIS) is India’s national standards body and functions under the Bureau of Indian Standards Act, 2016. The notification refers to Rule 15(1), of the Bureau of Indian Standards Rules, 2018, which allows BIS to establish, reaffirm, amend, revise or withdraw Indian Standards after consulting the relevant stakeholders. Under Rule 15(2) these changes are formally notified through the Official Gazette. The wider Rules also distinguish a standard from a compulsory legal requirement. Rule 24 states that Indian Standards are generally voluntary and become binding when a contract stipulates them, legislation refers to them, or a specific government order makes them mandatory. BIS similarly explains that compulsory use of the Standard Mark for covered products is directed through Quality Control Orders (QCOs). This means businesses must complete a second-level applicability check. A standard appearing in this notification is established and available for adoption, but mandatory certification cannot be inferred from this document alone. A relevant QCO, sectoral law, licence condition, procurement specification, contract or other binding instrument may still require compliance in a particular case. Scope and Applicability The notification relates to nine specifically mentioned standards instead of one comprehensive compliance system for the entire industry. The immediate issue that the notification deals with is the setting up of the standards specified and, in case of four standards, their coexistence with earlier versions followed by their withdrawal. Stakeholder or Activity Connection with the Notification Main Review Point Chemical manufacturers and users p-Toluidine, o-Toluidine, chlorosulphonic acid and hexane Identify the applicable specification or safety-code edition Animal-feed manufacturers and suppliers Monocalcium phosphate, animal feed grade Review IS 19887:2026 and any separate feed-law or contractual requirements Homoeopathic product manufacturers and laboratories Mother tinctures, Echinacea extract and biotherapeutic products Review the applicable test, specification or handling standard Traditional-medicine product businesses Echinacea angustifolia whole plant Review IS 19900:2026 where relevant to material specifications or procurement Testing laboratories Test methods and specifications may affect methods, scope and customer requirements Obtain the complete standard before changing a method or report format Procurement and contract teams Standards may be incorporated into tenders or supply agreements Verify the edition and transition language used in each contract Existing BIS licensees or applicants A revised standard may affect certification documentation if a scheme or licence covers it Check product-specific BIS directions separately, this notice gives no certification process The Gazette does not reproduce the technical clauses of the nine standards. It therefore does not provide product grades, sampling rules, test values, marking requirements, packaging conditions, laboratory methods or acceptance criteria. Those details must be taken from the official text of each relevant Indian Standard and any separately applicable legal instrument. What the BIS Indian Standards Notification 2026 Has Changed The latest BIS notification covers nine standards established in 2026, all carrying the same establishment date. Of these, four are revised versions of existing standards and will run alongside the older editions for six months before those editions are withdrawn. The other five are new standards, with no earlier versions listed for withdrawal. IS 5647 has moved from the 2003 first revision to the 2026 second revision. IS 5649 has moved from the 2003 second revision to the 2026 third revision. IS 6156 has received its first revision, replacing the 1971 code after the transition. IS 10870 has received its first revision, replacing the 1984 code after the transition. Five standards numbered IS 19887, IS 19897, IS 19898, IS 19900 and IS 19901 have been established without a predecessor identified in the schedule. Compliance Area Earlier Position Identified in the Notification New Position Relevant Date Business Meaning p-Toluidine specification IS 5647:2003, first revision IS 5647:2026, second revision New edition established 3 August 2026, old edition withdrawn 3 February 2027 Specifications and documents referencing the old edition should be reviewed o-Toluidine specification IS 5649:2003, second revision IS 5649:2026, third revision Same transition dates Quality, supply and testing references may need edition control Chlorosulphonic acid safety code IS 6156:1971 IS 5649:2026, third revision Same transition dates Safety systems should be compared with the revised code Hexane safety code IS 10870:1984 IS 10870:2026, first revision Same transition dates Handling and safety documentation should be checked against the new edition Five additional subjects No predecessor listed Five 2026 standards established 3 August 2026 Businesses should assess whether a newly available standard is relevant to products, tests or handling practices The notification does not provide a clause-by-clause comparison. Any statement about changed limits, test methods or safety controls would require the full earlier and 2026 standard texts. Nine Indian Standards Established by BIS S. No. 2026 Indian Standard Subject Status shown in notification 1 IS 5647:2026 p-Toluidine- Specification (Second Revision) Revises IS 5647:2003 2 IS 5649:2026 o-Toluidine- Specification (Third Revision) Revises IS 5649:2003 3 IS 6156:2026 Chlorosulphonic Acid- Code of Safety (First Revision) Revises IS 6156:1971 4 IS 10870:2026 Hexane- Code of Safety (First Revision) Revises IS 10870:1984 5 IS 19887:2026 Monocalcium Phosphate, Animal Feed Grade- Specification No earlier standard listed 6 IS 19897:2026 Homoeopathic Mother Tinctures (Hydro-Alcoholic Extracts)- Methods of Test No earlier standard listed 7 IS 19898:2026 Echinacea Angustifolia Hydro-Alcoholic Extract for Use in Homoeopathy- Specification No earlier standard listed 8 IS 19900:2026 Echinacea Angustifolia DC. Whole Plant for Use in Traditional Medicine- Specification No earlier standard listed 9 IS 19901:2026 Safe Handling of Biotherapeutic Products Used in Homoeopathy- Guidelines No earlier standard listed Revised Standards and Concurrent Validity The four older standards do not disappear on 3 August 2026. The Gazette expressly permits them to remain in force concurrently with the 2026 editions until 3 February 2027. This period allows users to manage edition changes, although the notification does not prescribe a detailed migration procedure. New standard Older standard running concurrently Concurrent period ends Scheduled withdrawal IS 5647:2026 IS 5647:2003 3 February 2027 3 February 2027 IS 5649:2026 IS 5649:2003 3 February 2027 3 February 2027 IS 6156:2026 IS 6156:1971 3 February 2027 3 February 2027 IS 10870:2026 IS 10870:1984 3 February 2027 3 February 2027 Concurrent validity does not automatically answer which edition a particular buyer, licence, tender or contract accepts. Users should read the controlling document. If it names an edition, changing that reference may require buyer approval, a contract amendment, updated certification directions or another formal action. New Standards with No Earlier Version Listed For IS 19887:2026, IS 19897:2026, IS 19898:2026, IS 19900:2026 and IS 19901:2026, the columns for an earlier standard and withdrawal date state “NA.” This means the notification does not identify a predecessor for withdrawal. It should not be expanded into a claim that no technical, pharmacopoeial, sectoral or contractual requirements existed previously. The five entries cover: animal-feed grade monocalcium phosphate, test methods for homoeopathic mother tinctures that are hydro-alcoholic extracts, an Echinacea angustifolia hydro-alcoholic extract specification for homoeopathic use, an Echinacea angustifolia DC. whole-plant specification for traditional-medicine use, and guidelines for safe handling of biotherapeutic products used in homoeopathy. Businesses in these fields should map the new standards against existing product specifications, laboratory procedures, pharmacopoeial references, supplier agreements and applicable sectoral laws. That exercise is a practical recommendation, not an express duty created by this Gazette notification. Implementation Timeline and Withdrawal Dates Event Date Affected parties Practical action Establishment of all nine standards 3 August 2026 Users of the listed standards Identify relevant standards and obtain the correct official edition Notification issued 5 August 2026 All stakeholders Record the reference in regulatory trackers Notification published in the Gazette 12 August 2026 All stakeholders Verify the published schedule and dates Concurrent running of four old editions ends 3 February 2027 Users of IS 5647, IS 5649, IS 6156 and IS 10870 Complete edition review before withdrawal Four older standards withdrawn 3 February 2027 Manufacturers, laboratories, procurement and safety teams using those editions Stop relying on the withdrawn edition unless another controlling instrument requires specific treatment No separate compliance deadline is given for the five standards with “NA” in the withdrawal columns. The notification also gives no filing window, application date, fee-payment date or certification transition process. Does This Notification Make BIS Certification Mandatory? No. The notification itself does not direct manufacturers to obtain a BIS licence, Certificate of Conformity, registration or Standard Mark. It establishes Indian Standards and sets concurrent-running and withdrawal dates for four older editions. This conclusion is limited to the document reviewed. Mandatory status must be checked separately because an Indian Standard may become binding through: a Quality Control Order or another specific government order, a reference in legislation or subordinate legislation, a licence, regulatory approval or scheme condition, a tender or procurement requirement, a customer or supply contract, or an existing BIS certification scheme that applies to the product. Before making or marketing a product as “BIS compliant,” businesses should verify both technical conformity and the legal basis for any required certification or marking. Establishment of a standard alone is not permission to use the BIS Standard Mark. Technical and Testing Considerations The Gazette only sets out the standard names and dates. It does not explain what businesses need to follow under each standard in practical terms. Details such as sample size, purity limits, testing equipment, storage conditions, packaging, labelling, quality checks and inspection schedules are not covered in the notification. The appropriate technical review should therefore begin with the full standard: Product specifications: Compare raw materials, grades, test parameters, acceptance criteria, packing and marking clauses, where included in the official standard. Methods of test: Confirm whether laboratories have the method, equipment, reference materials, calibration controls and competent personnel needed for the relevant tests. Codes of safety: Compare handling, storage, process-safety and emergency documentation with the revised code, without assuming the Gazette itself states particular controls. Guidelines: Determine how the guidance connects with internal procedures and any independently binding health, drug, safety or environmental law. Laboratories should not revise an accredited or approved method solely from the standard’s title. They should examine the full method and then follow the applicable accreditation, regulator, customer and change-control requirements. Impact on Businesses The immediate impact is document and edition control. The deeper effect will depend on what changed inside each standard and whether another binding instrument incorporates it. Chemical manufacturers, users and safety teams Businesses dealing with p-Toluidine, o-Toluidine, chlorosulphonic acid or hexane should identify where the older editions appear in specifications, safety procedures, customer approvals, testing plans and purchase orders. The long age of the earlier safety codes 1971 and 1984, makes a structured comparison with the 2026 revisions especially sensible, but the nature of the revisions cannot be inferred from age alone. Animal-feed businesses Manufacturers and suppliers of animal-feed grade monocalcium phosphate now have IS 19887:2026 listed as an established specification. They should examine whether customers, tenders or regulators adopt it. The notification does not itself amend feed law, prescribe certification or state product-compliance deadlines. Homoeopathy and traditional-medicine stakeholders The five standards in this group address test methods, Echinacea material and extracts, and safe handling of biotherapeutic products. Manufacturers, laboratories and quality teams may need to compare them with existing pharmacopoeial, manufacturing, laboratory and handling controls. No claim should be made that the Gazette replaces drug-law requirements. Laboratories and procurement teams Laboratories may need to review their testing methods, equipment, staff training, and accreditation scope once they go through the full standards. Procurement teams should also be clear about which edition they are accepting during the transition period. Mixing test reports or product specifications based on different editions can create confusion, so each case should be checked before acceptance. Stakeholder Immediate Impact Possible Operational or Cost Effect Priority Concern Manufacturers Identify relevant standards and editions Document updates, testing review or process changes may be needed Do not assume mandatory status without checking the controlling instrument Testing laboratories Obtain and compare the 2026 methods or specifications Possible method, equipment, training or accreditation review Use the correct edition and approved change process Safety and EHS teams Review revised chemical-safety codes Procedure and training updates may follow Compare actual clauses before changing controls Procurement teams Update standard references where appropriate Supplier communication and contract changes State accepted editions during the transition Existing licence holders or applicants Check whether BIS issues product-specific transition directions Testing and documentation costs may arise Do not treat the Gazette as the complete certification instruction Benefits for Businesses The standards can provide a common technical reference across suppliers, buyers, laboratories and operational teams. Likely benefits, subject to the content and adoption of each standard, include: clearer edition control for chemical specifications and safety codes, a current reference point for product testing and procurement, more consistent communication of material or product requirements, structured methods for laboratory work where IS 19897:2026 applies, a defined specification for animal-feed grade monocalcium phosphate, recognised references for Echinacea material and hydro-alcoholic extract, and a handling guideline for biotherapeutic products used in homoeopathy. These are potential standardisation benefits. The notification does not guarantee regulatory approval, product quality, market acceptance, lower costs or commercial returns. Challenges and Cost Implications The Gazette states no fee or implementation cost. Any cost will depend on the detailed differences between editions and the way a business uses the standard. Possible cost drivers include purchasing official standards, technical gap analysis, laboratory method review, new equipment or reference materials, staff training, supplier qualification, revised documentation and contract amendments. Certification or laboratory costs should be added only if a separate mandatory or voluntary conformity-assessment route actually applies. MSMEs may need to prioritise the documents that carry the greatest legal, customer or safety relevance. A staged review can begin with binding contracts and regulated products, followed by internal specifications and voluntary improvement work. Best Practices During the Transition Keep a controlled register showing each old and new standard number, issue year, owner and affected process. Obtain the official standard text rather than relying on summaries or the Gazette title. Compare clauses before changing a product specification, test method or safety procedure. Check QCOs, sectoral laws, licences, tenders and contracts separately for mandatory status. Record which edition applies to each batch, test report, purchase order and customer specification during concurrent running. Ask customers or certification bodies to clarify edition acceptance where the controlling document is unclear. Complete internal approval, training and document control before 3 February 2027 for the four withdrawing editions. Preserve evidence of the review and the reason for each adopted change. Common Risks to Avoid Treating 12 August 2026, the publication date, as the standards’ establishment date. Claiming that all nine standards are compulsory merely because they were published in the Gazette. Claiming that the five “NA” entries had no earlier regulatory or technical requirements of any kind. Using the title of a standard as a substitute for reading its technical clauses. Assuming that concurrent running lets every licence holder or supplier choose either edition without checking the controlling terms. Continuing to cite the four older editions after 3 February 2027 without reviewing the effect of withdrawal. Using or advertising the BIS Standard Mark without the required authorisation. Inventing penalties, fees, application steps or testing deadlines that do not appear in the notification. What Businesses Should Do Next 1. Confirm applicability. Match products, materials, tests and handling activities against the nine exact standard titles. 2. Obtain the relevant standards. Use official BIS copies of both the current and earlier editions where comparison is required. 3. Check mandatory status separately. Review QCOs, sector laws, licences, contracts and tender conditions. 4. Perform a clause-level comparison. Identify technical, testing, documentation, safety, packaging or marking changes actually present in the standard. 5. Prepare transition controls. Assign owners and complete necessary updates before 3 February 2027 for the four older editions scheduled for withdrawal. 6. Coordinate external requirements. Confirm expectations with customers, laboratories, certification bodies and suppliers where their approval or action is needed. 7. Maintain evidence. Record the applicable edition, assessment, decisions, approvals, training and revised documents. Action Responsible Team Relevant Date Expected Outcome Determine which standards apply Regulatory, quality and product teams Immediate Clear scope Verify whether adoption is voluntary or binding Legal and regulatory teams Before changing compliance claims or certification plans Correct legal position Compare old and new editions Technical, laboratory and safety teams Before 3 February 2027 for revised standards Evidence-based transition plan Update controlled documents and contracts where required Quality, EHS, procurement and legal teams Before the relevant edition change Consistent documents and supplier expectations Monitor product-specific BIS directions Regulatory and certification teams Ongoing Timely response to any separate implementation instruction How Corpseed Can Help? Corpseed can support businesses that need to understand how the nine standards affect their products, testing arrangements, contracts or certification position. The scope should begin with applicability, because this notification does not make certification mandatory by itself. Applicability assessment for the relevant Indian Standard and product category Review of QCOs and other instruments that may make a standard binding Old-versus-new standard gap assessment using the official editions supplied for review Product and technical-document compliance review Coordination support for laboratory testing where testing is relevant Review of certification pathways and application documentation where a BIS scheme applies Transition planning for standards withdrawn on 3 February 2027 Ongoing regulatory and standard-edition monitoring support A BIS certification consultant should first confirm whether certification is mandatory, voluntary or not applicable. Corpseed assists manufacturers and other stakeholders with this assessment and with the matching product compliance services, without promising certification, approval or a fixed regulatory outcome. Businesses using any of the nine standards may contact Corpseed to speak with a BIS certification consultant about a document-specific applicability and transition review. Key Takeaways BIS notification Ref. HQ-PUB013/1/2020-PUB-BIS (1583) establishes nine Indian Standards from 3 August 2026. Four 2026 revisions will run concurrently with their earlier editions until those older standards are withdrawn on 3 February 2027. Five standards have no predecessor identified in the schedule. The BIS Indian Standards notification 2026 covers chemicals, chemical safety, animal feed, homoeopathy and traditional medicine. The notification is dated 5 August and was published on 12 August 2026. It does not itself impose certification, registration, testing or licensing. Mandatory status must be checked through QCOs, legislation, contracts and other controlling instruments. Affected businesses should obtain the full standards and compare actual clauses before changing operations. Transition planning is most urgent for IS 5647, IS 5649, IS 6156 and IS 10870.

Subject

Summary: The Bureau of Indian Standards (BIS) has notified five BIS medical device standards in 2026 covering microwave therapy apparatus, photodynamic therapy and diagnostic apparatus, home light therapy apparatus, and medical endoscopes and endotherapy apparatus. The standards were developed on 3 August 2026. The notification is dated 5 August 2026 and was published in the Gazette of India on 12 August 2026 under reference HQ-PUB013/1/2020-PUB-BIS (1584). For three revised standards, BIS has allowed the earlier editions to remain in force concurrently until 3 February 2027. The other two entries are shown as new standards with no earlier standard or withdrawal date listed. Manufacturers, importers, testing laboratories, product designers, quality control units, and buyers involved with the equipment listed above need to determine the relevant standard and evaluate the technical documentation during the transition. The notification sets and revokes the standards but does not itself indicate that BIS certification or the Standard Mark is mandatory. Notification at a Glance Particular Verified details Issuing authority Bureau of Indian Standards, Department of Consumer Affairs Date of establishment 3 August 2026 for all five standards Governing provision Rule 15(1) of the Bureau of Indian Standards Rules, 2018 Sector and products Medical electrical equipment; microwave therapy; photodynamic therapy and diagnosis; home light therapy; endoscopes and endotherapy devices Main stakeholders Manufacturers, importers, laboratories, designers, quality and regulatory teams, distributors and institutional purchasers connected with the listed equipment Core development Five standards established; three older editions scheduled for withdrawal Main transition date 3 February 2027 for the three superseded standards Nature of requirement Standard-establishment and withdrawal notification; compulsory certification is not expressly created by this notification Fees or penalties in this notification Not expressly specified The Regulatory Framework BIS is India's national standards body. The present notification was issued under Rule 15(1) of the Bureau of Indian Standards Rules, 2018. Rule 15 deals with the preparation, publication, revision, and withdrawal of Indian Standards. Schedule is the part of this notification that works: it mentions the new edition, its date of adoption, the previous edition, if any, and the date of its withdrawal. This notification should not be confused with a Quality Control Order (QCO). BIS guidance explains that product certification is generally voluntary. At the same time, the Central Government can make conformity and use of the Standard Mark compulsory through a QCO or another applicable legal instrument. No QCO, mandatory Standard Mark direction, license condition, certification scheme, enforcement provision, or penalty appears in this five-page notification. The listed standards draw on publications of the International Electrotechnical Commission (IEC) and the International Organization for Standardization (ISO). The Gazette identifies three IEC-based standards for medical electrical equipment and two ISO-based standards for endoscopes. The technical text of those standards is not reproduced in the notification, so clause-level product requirements must be checked against the complete standards themselves. Scope and Applicability The notification applies only to the five stated standards, not to all devices or all types of electrical medical equipment. Applicability depends on whether the product falls within the scope of any of the mentioned standards. Product or standard group Covered by this notification? Relevant condition Main review area Product or standard group Yes IS 13450 (Part 2/Sec 6): 2026 Basic safety and essential performance requirements in the complete standard Photodynamic therapy and photodynamic diagnosis equipment Yes IS 13450 (Part 2/Sec 75): 2026 Product classification, design and technical evidence against the new standard Photodynamic therapy and photodynamic diagnosis equipment Yes IS 13450 (Part 2/Sec 75): 2026 Scope fit and safety/performance evidence for home-use light therapy equipment Medical endoscopes and endotherapy devices Yes IS 15732 (Part 1): 2026 and/or IS 15732 (Part 4): 2026, depending on the issue assessed General requirements and maximum width of insertion portion Medical devices outside the titles and scopes listed above Not established by this notification Another Indian Standard or regulatory instrument may apply General requirements and maximum width of insertion portion The document does not mention any exemptions, risk classifications, turnovers, locations, or special considerations for MSMEs. In addition, it does not state that all manufacturers, importers, or distributors are obliged to make an application immediately. These considerations depend on the complete standard and the related medical device or BIS instrument. What Has Changed BIS established five standards on the same date. Three are revised editions with six months during which the old and new versions remain in force together. Two are listed without a predecessor. Compliance area Earlier position New position Relevant date Business meaning Microwave therapy equipment IS 13450 (Part 2/Sec 6): 2018, based on IEC 60601-2-6: 2012 IS 13450 (Part 2/Sec 6): 2026, based on IEC 60601-2-6:2012 with Amendments 1 and 2, consolidated and modified New edition established 3 August 2026; old edition withdrawn 3 February 2027 Review changes and plan migration before withdrawal Photodynamic therapy and diagnosis equipment No earlier standard listed IS 13450 (Part 2/Sec 75): 2026 Established 3 August 2026 Assess whether products fall within this newly listed section Home light therapy equipment No earlier standard listed IS 13450 (Part 2/Sec 83): 2026 Established 3 August 2026 Assess scope and align relevant technical records Endoscope general requirements IS 15732 (Part 1): 2018 / ISO 8600-1:2015 IS 13450 (Part 2/Sec 83): 2026 New edition established 3 August 2026; old edition withdrawn 3 February 2027 General requirements documentation may need updating Endoscope insertion-portion width IS 15732 (Part 4): 2021 / ISO 8600-4:2014 IS 15732 (Part 4): 2026 / ISO 8600-4:2023 New edition established 3 August 2026; old edition withdrawn 3 February 2027 Review the method and records used to determine maximum insertion width The notification does not provide a redline or clause-by-clause comparison. A business should not assume the changes are limited to the amended years shown in the titles. A proper gap review requires the complete old and new standards. Detailed Standard-Wise Analysis IS 13450 (Part 2/Sec 6): 2026 - Microwave Therapy Equipment This is the first revision of the Indian Standard that contains specific requirements for the basic safety and essential performance of microwave therapy equipment. BIS identifies it with IEC 60601-2-6:2012, Amendment 1:2016, and Amendment 2:2022, in consolidated form, with modifications. Indian Standards of 2018 and their revisions until 2026 will remain relevant until 3rd February 2027. For businesses using the 2018 standard, they can check for changes in the technical specifications between the two versions of the standard and identify which designs, tests, risks, and products will require modification. The notice provides no list of modified clauses and testing. IS 13450 (Part 2/Sec 75): 2026 - Photodynamic Therapy and Diagnosis Equipment This standard address particular requirements for the basic safety and essential performance of photodynamic therapy and photodynamic diagnosis equipment. It is identified with IEC 60601-2-75:2017 and Amendment 1:2023 in consolidated, modified form. The schedule has marked NA for both the earlier standard as well as the withdrawn date of the same. Based on the information provided, the BIS has not identified any predecessor that runs parallel to it. However, this is not conclusive evidence of the absence of any other general/collateral/product standard which may be applicable. IS 13450 (Part 2/Sec 83): 2026 - Home Light Therapy Equipment This new entry covers particular requirements for the basic safety and essential performance of home light therapy equipment. It is linked to IEC 60601-2-83:2019 and Amendment 1:2022 in consolidated, modified form. Unlike Section 75, the Gazette has no precedent for this standard and no withdrawal date. It would be best for manufacturers and importers to ensure that the product falls under the jurisdiction of Section 83 first. This is because the title alone must not determine whether equipment belongs to this category. IS 15732 (Part 1): 2026 - General Requirements for Endoscopes IS 15732 (Part 1): 2026 is the second revision of the general requirements standard for medical endoscopes and endotherapy devices. It adopts ISO 8600-1:2025. The earlier IS 15732 (Part 1): 2018, based on ISO 8600-1:2015, remains in force until 3 February 2027. The heading is rather broad and could influence product specifications and technical documentation across a range of endoscopes and endotherapy devices. The Gazette does not include the new technical provisions. Companies will have to obtain the complete 2026 standard in order to make an accurate comparison. IS 15732 (Part 4): 2026 - Maximum Width of the Insertion Portion IS 15732 (Part 4): 2026 is the second revision of the method for determining the maximum width of the insertion portion of medical endoscopes and endotherapy devices. It adopts ISO 8600-4:2023. The earlier 2021 Indian Standard, based on ISO 8600-4:2014, is scheduled to be withdrawn on 3 February 2027. All concerned teams, engineering, metrology, quality, and testing, should review whether the new procedure modifies any procedures, equipment, acceptance documentation, or product dimensions. Since no figures, tolerances, or procedures are provided in the notice, none should be derived from the title. Meaning of CSV, MOD, and Revision Labels The standard titles contain technical publication labels that help readers identify the source edition but do not replace the full Indian Standard. CSV means consolidated version. IEC explains that a CSV merges a publication and its amendments into a single document. MOD indicates that the Indian Standard is a modified adoption of the referenced international standard. Product teams should therefore use the Indian Standard and identify the national modifications rather than relying only on the IEC text. The first and second revisions identify the revision status of the Indian Standard. They do not, by themselves, describe which clauses changed. NA in the predecessor and withdrawal columns means the schedule lists no earlier standard for withdrawal for that entry. Implementation Timeline/Norms Event Date Affected standards Required or practical action Establishment of all five standards 3 August 2026 All five new standards Treat this as the formal establishment date recorded by BIS Notification date 5 August 2026 Entire notification Record the document date separately from establishment and publication Gazette publication 12 August 2026 Entire notification Use the official Gazette copy for the publication record Concurrent-validity period 3 August 2026 to 2 February 2027 Section 6, Part 1 and Part 4 revised standards Compare editions and plan transition where applicable Withdrawal of three earlier standards 3 February 2027 IS 13450 (Part 2/Sec 6):2018; IS 15732 (Part 1):2018; IS 15732 (Part 4):2021 Stop treating the withdrawn editions as current after the withdrawal date, subject to any separately applicable regulatory directions It is clear from The Gazette that February 3, 2027, is not mentioned as a universal certification deadline. These are just withdrawal dates of three identified standards. Any conversion requirement arising from a license, QCO, purchasing agreement, or medical device approval should be assessed according to the instrument that creates the requirement. Old vs. New Requirements The authenticated comparison is restricted to edition identification, international publication citation, and transfer date due to the absence of the technical content of the standards in the Gazette. Standard Older edition 2026 edition Verified transition Microwave therapy equipment IS 13450 (Part 2/Sec 6):2018; IEC 60601-2-6:2012 Includes IEC Amendments 1:2016 and 2:2022 in CSV form; MOD Concurrent until 3 February 2027 Endoscope general requirements IS 13450 (Part 2/Sec 6):2018; IEC 60601-2-6:2012 IS 15732 (Part 1):2026; ISO 8600-1:2025 Concurrent until 3 February 2027 Maximum insertion-portion width IS 15732 (Part 4):2021; ISO 8600-4:2014 IS 15732 (Part 4):2026; ISO 8600-4:2023 Concurrent until 3 February 2027 An old-versus-new comparison table cannot detail the technical differences between the two editions because access to both versions is unavailable. Does This Notification Make BIS Certification Mandatory? This notification does not impose any mandatory BIS certification. This notification issued by BIS is based on Rule 15(1). This rule involves both the establishment of new standards and the discontinuation of existing ones. There is nothing in this notification about the compulsory use of the standard mark. Neither is there any BIS license, conformity assessment scheme, nor any penalty. The BIS's formal guidance on QCO distinguishes between voluntary and mandatory certification through the QCO process. Hence, businesses are required to perform the second check with regard to any QCO, license condition, procurement requirement, regulatory requirement in connection with medical devices, or other legal document that may reference these standards. However, the impact depends on the instrument itself and is not implied by this notice. Impact on Businesses The direct impact on business will be to determine whether a listed standard is applicable and, for revised standards, whether existing technical data remain applicable when the older edition is phased out. Manufacturers and Product Designers Map each model and variant to the relevant standard instead of applying the notification to the entire product portfolio. Obtain the complete 2026 standard before changing product design, specifications, labels, or test plans. Compare old and new clauses for the three revised standards and document the effect on design inputs, risk controls, and verification evidence. For Sections 75 and 83, conduct a fresh scope assessment because no predecessor is listed. Importers, Distributors and Institutional Purchasers Ask suppliers which edition supports the product's technical evidence and whether transition work is planned. Review contracts, tender specifications, and purchase requirements that cite an older standard. Avoid describing the product as legally required to hold BIS certification solely because the standard appears in this notification. Laboratories and Quality Teams Confirm whether test methods, equipment, measurement procedures, and report templates align with the new edition. The two different editions need to be clearly separated during concurrent validation. Include the standard's number and year in the report to avoid confusion. MSMEs and Startups There is no specific transition period or exemption given for MSMEs and startups. Smaller business establishments will find it more challenging to meet standards, conduct gap assessments, and update technical files. Stakeholder Immediate impact Likely operational or cost effect Priority concern Manufacturers Standards mapping and edition comparison Engineering review and possible retesting Product scope and transition plan Importers Supplier evidence review Document updates and supplier coordination Product scope and transition plan Laboratories Method and capability assessment Document updates and supplier coordination Exact requirements of the new edition Purchasers Specification update Tender and contract revision Exact requirements of the new edition MSMEs and startups Applicability check Proportionately higher review cost Focus effort only on relevant products These cost effects are likely implications, not charges imposed by the Gazette. No testing fee, certification fee, or compliance cost is specified in the notification. Benefits for Businesses This amendment ensures companies have a well-defined history of the editions and transition period for three standards. Some possible advantages are: an updated Indian reference based on recent IEC or ISO publications; proper identification of standards belonging to new classes of products such as photodynamic therapy and light therapy equipment; and an opportunity to compare three obsolete editions before withdrawal. more consistent edition references in design, testing, procurement, and quality records; an opportunity to remove outdated specifications from contracts and technical files; and Better coordination among engineering, regulatory, quality, and purchasing teams. These are the practical advantages of proper standards management. The announcement will not ensure any certification, regulation, market access, product safety, or commercial success. Challenges and Cost Implications The main problem here is that the standards are included in the Gazette, but the technical information contained in them is not. A good assessment will require comparing the standards with earlier versions. Possible short-term cost issues might include engineering review, acquisition of standards, lab capability review, supplier coordination, document revision, and testing as necessary according to the gap assessment process. There might also be recurring costs due to the different controls required by the revised method. The quantity or rate cannot be given from this source. Two additional items will require careful consideration. In the absence of an older standard, teams may have to develop a scope and evidence map rather than rely on a migration file. At the same time, teams must determine if any other standards still apply. Risks and Consequences of Non-Compliance There is no punishment prescribed for non-compliance with the notification. Therefore, it would be incorrect to say that failure to meet the deadline of 3 February 2027 will result in a penalty or recall. However, practical risks may emerge if the company continues to reference the withdrawn standard in testing reports, tenders, contracts, and technical specifications. If other binding documents or licenses require the use of the existing Indian Standard, then the consequences of migration should be evaluated separately. Best Practices Maintain a controlled standards register with the exact part, section, year, establishment date, and withdrawal date. Assign an owner for each affected product family and record the scope decision. Obtain the full standards and use a traceable clause-comparison method for revised editions. Separate legal requirements from voluntary technical improvement and customer-specific requirements. Record which external instrument, if any, makes conformity or certification mandatory. Update supplier questionnaires, purchase specifications, and laboratory instructions with the correct edition year. Retain approval for each change to design, testing, or documentation. Common Mistakes or Risks to Avoid Treating the Gazette publication date as the date of establishment. Calling 3 February 2027 a universal certification deadline rather than a withdrawal date for three standards. Assuming “NA” means no other standard or regulation can apply. Using only the referenced IEC or ISO document without checking modifications in the Indian Standard. Claiming BIS certification is mandatory without locating the instrument that creates that duty. Describing technical changes without comparing the complete old and new standards. Applying one listed standard to all medical devices based only on a broad product description. Future Outlook The only confirmed future action in the notification is the withdrawal of three earlier standards on 3 February 2027. No future review, amendment, certification deadline, or additional phase is announced. Companies must keep an eye on BIS and relevant sectoral regulators for manuals, implementation guidance, QCOs, license directions, and any other notices. Monitoring is a practical suggestion and not an action to be taken in the future. What Businesses Should Do Next Priority Action Responsible team Relevant date Expected outcome 1 Identify products potentially covered by the five standards Responsible team Begin promptly Verified product-to-standard map 2 Obtain the complete applicable 2026 standards Responsible team Before technical comparison Authoritative technical source available 3 Compare old and new editions for Sections 6 and Parts 1 and 4 Engineering, quality and laboratory teams Before 3 February 2027 Documented gap assessment and migration plan 4 Conduct fresh scope reviews for Sections 75 and 83 Regulatory and engineering teams Begin promptly Recorded applicability decision 5 Check separately for QCOs, license terms, and sectoral obligations Legal and regulatory teams Before claiming mandatory status Correct legal basis for each obligation 6 Update specifications, reports, and supplier documents Quality, procurement and document-control teams In line with the verified transition plan Consistent edition references 7 Preserve evidence of decisions and approvals Document-control owner Ongoing Traceable standards-management record How Can Corpseed Help? Corpseed supports manufacturers, importers, and other businesses affected by the 2026 BIS medical-device standards update. The support is tailored to the product, applicable standard, and actual compliance requirements. 1. Checking Which BIS Standard Applies Corpseed can help determine whether the new standards cover a particular medical device. Review the product’s purpose, design, and technical features. Identify the relevant BIS standard. Check different models and product variants. Avoid applying an unrelated standard to the product. 2. Mapping Products to the Correct Standards A business may manufacture or import several devices. Each product must be assessed separately. Prepare a product-to-standard mapping. Separate covered products from products outside the notification. Identify the correct standard number, part, section, and year. Create a clear reference for regulatory and quality teams. 3. Comparing Old and New Standards Three earlier standards will remain valid only until 3 February 2027. Corpseed can support a structured comparison when the complete editions are available. Compare the old and revised standards. Identify changes affecting the product. Highlight possible gaps in existing technical records. Prepare a practical transition plan. Help teams prioritize actions before the older standard is withdrawn. 4. Reviewing Technical Documents and Test Reports Technical documents should mention the correct standard and edition. Review product specifications and technical files. Check test reports and supporting records. Identify outdated or incorrect standard references. Review whether available evidence supports the applicable standard. Suggest document updates where necessary. 5. Supporting Product Testing Testing should be arranged only after confirming that it is required and identifying the correct standard. Help determine whether additional testing may be needed. Identify the relevant testing scope. Support coordination with a suitable laboratory. Review whether test reports mention the correct standard and edition. Help organize testing records for future reference. 6. Checking BIS Certification and QCO Applicability The 2026 notification establishes and withdraws standards. It does not, by itself, make BIS certification compulsory. Corpseed can help businesses: Check whether a separate Quality Control Order applies. Review whether a BIS license or Standard Mark is required. Examine other applicable certification or regulatory conditions. Separate voluntary standards from mandatory requirements. Avoid unnecessary certification applications or unsupported compliance claims. 7. Planning the Transition and Ongoing Compliance Businesses using the three older standards should prepare for their withdrawal on 3 February 2027. Create a product-specific transition plan. Assign responsibilities to regulatory, quality, and technical teams. Update internal standards registers and compliance records. Review supplier and laboratory documents. Monitor relevant BIS and regulatory updates. Maintain clear records of compliance decisions and completed actions. A medical device regulatory consultant helps connect the correct product, technical standard, and legal requirement. Corpseed can support businesses dealing with microwave therapy equipment, photodynamic therapy and diagnostic equipment, home light therapy equipment, medical endoscopes, and endotherapy devices. Businesses may contact Corpseed for a document-specific assessment and practical support with medical-device compliance. Certification, approval, or a fixed regulatory result is not guaranteed.

Subject

Summary: The Hallmarking of Gold Jewellery and Gold Articles (Third Amendment) Order, 2026, is an amendment to the existing law on mandatory gold hallmarking in India and affects all jewellers, gold dealers, manufacturers, and retailers operating in India. This order, issued by the Ministry of Consumer Affairs, Food and Public Distribution, on August 3, 2026, and published in the Gazette of India on August 6, 2026, amends the list of districts for which BIS hallmarking of gold jewellery is mandatory. If your business sells, manufactures, or trades gold jewellery or gold artefacts, this update could change whether hallmarking is now mandatory in the district where you operate, and getting it wrong can mean penalties, seized stock, or a blocked BIS registration . Many businesses struggle to track ongoing changes like this one, which is exactly why working with an experienced gold hallmarking compliance consultant like Corpseed can help you stay ahead of the deadline rather than react to it after an inspection. Key Highlights of the Amendment The order is called the Hallmarking of Gold Jewellery and Gold Artefacts (Third Amendment) Order, 2026. It has been issued by the Central Government, through the Department of Consumer Affairs, Ministry of Consumer Affairs, Food and Public Distribution. It is issued under the Bureau of Indian Standards (BIS) Act, 2016, specifically Section 14(3) read with Sections 15(2), 15(3), 16, 17, and 25(3). The government consulted the Bureau of Indian Standards (BIS) before issuing this order, as required by law. The amendment replaces the entire Annexure (the district-wise list) of the original Hallmarking of Gold Jewellery and Gold Artefacts Order, 2020. The new Annexure lists districts, state by state and union territory by union territory, where hallmarking of gold jewellery and gold artefacts is mandatory. The order becomes effective immediately from its date of publication in the Official Gazette, i.e., August 6, 2026. This is the third amendment to the original 2020 Order. The principal order was notified on January 15, 2020, and was last amended on April 28, 2026 (S.O. 2117(E)), before this latest change. The order is signed by Richa Misra, Additional Secretary, on behalf of the Central Government. Businesses operating in any district newly added to the Annexure must ensure their gold jewellery and gold artefacts carry a valid BIS hallmark without delay. No transition period is separately specified in the order; compliance is expected from the date the order takes effect. The Regulatory Framework What Law Governs This Order? This order is made under the Bureau of Indian Standards Act, 2016 (Act No. 11 of 2016). In simple terms, this law empowers the Central Government and BIS to make hallmarking (a quality and purity certification mark) compulsory for certain goods, including gold jewellery and gold artefacts. The specific legal provisions used are: Section 14(3)- power to specify goods, articles, or products for compulsory hallmarking or certification. Section 15(2) and 15(3)- powers related to standard marks and certification schemes. Section 16- provisions dealing with hallmarking or certification requirements. Section 17- provisions on how compulsory marking is implemented. Section 25(3)- powers to make orders for goods or articles requiring compulsory certification. Who Is the Regulatory Authority? The Bureau of Indian Standards (BIS) is India's national standards body and the technical authority responsible for hallmarking. The Department of Consumer Affairs (under the Ministry of Consumer Affairs, Food and Public Distribution) is the administrative authority that issues the legal order making hallmarking compulsory in specified districts, after formally consulting BIS. Purpose and Scope The purpose of this framework is to ensure that gold jewellery and gold artefacts sold in India meet a guaranteed purity standard, verified and certified by a BIS hallmark. The scope of this particular amendment is limited to updating the list of districts where this requirement legally applies it does not change the hallmarking process, purity standards, or registration requirements themselves, which continue to be governed by the parent 2020 Order and BIS regulations. Industries Covered This order applies to: Gold jewellery manufacturers Gold artefact makers Jewellery retailers and showrooms Gold traders and wholesalers Jewellery exporters dealing in domestic sales. Any business that sells or supplies gold jewellery or gold artefacts to consumers in the districts listed in the Annexure What Has Changed? The core change made by this amendment is straightforward but important: the entire Annexure (district list) of the 2020 Order has been replaced with a new Annexure. Aspect Position Before This Amendment Position After This Amendment (2026) Governing Annexure Annexure as it stood after the amendment dated April 28, 2026 (S.O. 2117(E)) New Annexure substituted in full by this order (S.O. 4345(E)) District coverage Based on the earlier notified list Updated, state-wise and UT-wise list of districts as newly published Legal status Hallmarking mandatory only in previously listed districts Hallmarking mandatory in all districts now listed in the new Annexure Effective date N/A From the date of publication in the Gazette, i.e., August 6, 2026 Not sure which rule applies to your stock? Corpseed's BIS Registration experts can review your product line against the current Annexure in a single consultation.  Important Note: The order text itself does not describe the amendment as adding a fixed number of new districts it simply states that the previous Annexure "shall be substituted" with the new one. Businesses should check the new Annexure directly against their operating district to confirm applicability, rather than assuming their district's status has stayed the same. Which Districts Are Covered Under the New Annexure? The new Annexure lists districts across 26 states and union territories. Below is a quick-reference table of some of the major districts named in the official list, so you can quickly check whether a well-known city or district near you is covered. This is not the complete list; the notification spans dozens of districts per state, but it gives you a quick way to check the states and prominent districts most people search for. State / UT Prominent Districts Covered (as per the official Annexure) Delhi New Delhi, Central Delhi, East Delhi, North Delhi, South Delhi, West Delhi, North West Delhi, South East Delhi Maharashtra Mumbai City, Mumbai Suburban, Pune, Nagpur, Nashik, Thane, Aurangabad, Kolhapur Karnataka Bengaluru Urban, Mysore, Dakshina Kannada, Belagavi, Hubli-area (Dharwad) Tamil Nadu Chennai, Coimbatore, Madurai, Tiruchirappalli, Salem, Vellore Telangana Hyderabad, Rangareddy, Warangal Urban, Warangal Rural, Karimnagar West Bengal Kolkata, Howrah, Darjeeling, Hooghly, North 24 Parganas, South 24 Parganas Gujarat Ahmedabad, Surat, Vadodara, Rajkot, Bhavnagar, Kutch Rajasthan Jaipur, Jodhpur, Udaipur, Kota, Ajmer, Bikaner Uttar Pradesh Lucknow, Agra, Kanpur Nagar, Varanasi, Meerut, Ghaziabad, Prayagraj Punjab Amritsar, Ludhiana, Jalandhar, Patiala, Bathinda Andhra Pradesh Visakhapatnam, Guntur, Krishna, Kurnool, East Godavari Kerala Ernakulam, Thiruvananthapuram, Kozhikode, Thrissur, Kollam Madhya Pradesh Bhopal, Indore, Gwalior, Jabalpur, Ujjain Bihar Patna, Gaya, Bhagalpur, Muzaffarpur, Darbhanga Assam Kamrup Metro, Cachar, Jorhat, Nagaon, Dibrugarh-area (Tinsukia) Chandigarh Chandigarh Puducherry Puducherry, Karaikal Don't see your exact district above? The full Annexure covers many more districts within each of these states (and others, including Chhattisgarh, Goa, Haryana, Himachal Pradesh, Jammu & Kashmir, Jharkhand, Odisha, Tripura, and Uttarakhand). Since hallmarking applicability is district-specific and legally binding, always verify your exact district against the official Gazette notification rather than relying on general area names. If you're unsure how to read the Annexure or want direct confirmation for your business location, Corpseed's compliance team can check district applicability for you as part of a hallmarking compliance review. Implementation Timeline / Norms Effective Date: The order shall come into effect on August 6, 2026, which is the date of publication of this order in the Official Gazette. No such delay in the operation of the order has been provided for. Compliance Deadline: In view of the immediate operation of the order, businesses operating in districts covered by the new Annexure are required to comply with this date. Applicability: The order applies to any business dealing in gold jewellery or gold artefacts within a district named in the new Annexure. Required Actions: Check whether your operating district appears in the new Annexure. If it does, confirm your BIS hallmarking registration is active and valid. Ensure every piece of gold jewellery or gold artefact sold carries a genuine BIS hallmark (including a HUID). Update internal compliance checklists and staff training to reflect the new district status, if applicable. Maintain proper documentation proving hallmarking compliance in the event of an inspection. Why Was This Implemented? While the order itself is procedural (updating a district list), it fits into the Central Government's broader objective behind mandatory gold hallmarking, which includes: Consumer protection:  ensuring buyers of gold jewellery get exactly the purity they pay for. Standardisation:  bringing gold jewellery sold across India under a uniform, verifiable quality mark. Trade transparency:  reducing disputes between buyers and sellers over gold purity. Ease of doing business:  giving jewellers a clear, predictable national framework instead of inconsistent local practices. Progressive expansion:  gradually widening hallmarking coverage to more districts as BIS's registration and assaying infrastructure (Assaying & Hallmarking Centres) becomes available in those areas. Impact on Businesses Gold jewellery and articles manufacturers: Manufacturers whose factory is located in a new area covered under the Act shall ensure that all their products are hallmarked before being sold. Importers: Those importers who repack, relabel, and sell the gold jewellery within India shall ensure compliance with hallmarking laws. Exporters: In most cases, exporters dealing in export business to countries other than India are not much affected by the Act; however, in the event of any domestic sale in a covered district, they are affected by the Act. Brand owners and large jewellery chains: Multi-location brands need to map every showroom against the new Annexure and update store-level compliance status accordingly. MSMEs and small jewellers: Smaller businesses, which may have limited compliance bandwidth, face the greatest operational adjustment if their district is newly listed, as they must quickly arrange BIS registration and access to hallmarking. Startups entering the jewellery business: New entrants must build hallmarking compliance into their business plan from day one if operating in a listed district. Traders, distributors, and retailers: Anyone in the supply chain selling directly to consumers in a covered district must verify that stock received from suppliers is properly hallmarked. OEMs and job-work units: Units manufacturing on behalf of brands must ensure hallmarking is completed before goods are dispatched for sale. Service providers (repair, remaking, customisation): Businesses that alter or remake jewellery for customers should be aware that hallmarking obligations continue to apply to the finished product sold. The operational impact includes coordinating with AHCs for testing and marking; the legal impact includes potential penalties for non-compliance; the financial impact includes hallmarking and registration costs, the documentation impact includes maintaining hallmarking records, and the supply chain impact includes verifying hallmark status of goods received from vendors before resale. How Businesses Will Achieve Compliance? Check district applicability:  Compare your business location against the new Annexure published with this order. BIS Registration:  Apply for or renew your BIS hallmarking registration if your district is newly covered. Documentation:  Maintain proof of registration, hallmarking certificates, and HUID records for all stock. Testing and Assaying:  Get gold jewellery and artefacts tested and hallmarked through a BIS-recognised Assaying and Hallmarking Centre. Approvals:  Ensure all necessary BIS approvals are current before selling hallmark-required stock. Certification:  Confirm each piece carries the mandatory hallmark, including purity grade and HUID. Inspection Readiness:  Keep records organised so you can respond quickly if BIS or Legal Metrology officials inspect your premises. Renewals:  Track registration validity and renew before expiry to avoid a compliance gap. Reporting:  Maintain internal reporting on hallmarking status across all outlets and stock. Record Maintenance:  Preserve purchase and hallmarking records for the period required under BIS rules. Common Compliance Mistakes: Assuming an old district status still applies without checking the updated Annexure. Selling hallmarked stock while a fresh BIS registration application is still pending. Not training sales staff to check hallmark and HUID details before billing. Poor recordkeeping that makes it hard to prove compliance during an inspection. Practical Tip: Don't wait for an inspection to discover your district has been added to the mandatory list. Proactively verifying applicability, the moment an order is published protects your business from last-minute scrambling. Need this done for you? Corpseed handles BIS hallmarking registration end-to-end from checking district applicability to filing your application and tracking approval.  Benefits for Businesses Below are the key benefits businesses can gain by complying with BIS hallmarking requirements. Legal compliance with the BIS Act, avoiding penalties and enforcement action. Reduced risk of penalties, seizure of hallmarked stock, or business disruption. Greater consumer trust, since a BIS hallmark is a recognised assurance of gold purity. Stronger brand reputation in a market increasingly sensitive to authenticity. Business continuity, avoiding the risk of a stop-sale situation due to non-compliance. Better market access, since informed buyers and large retail partners prefer hallmarked jewellery. Operational clarity, with a single, verifiable national standard instead of inconsistent practices. Right Decision or Additional Burden? Mandatory hallmarking and its gradual district-by-district expansion are generally seen as a positive step for consumer protection and market credibility. Still, it does come with real costs for smaller businesses. Strengths: The initiative builds consumer confidence in the quality of gold jewellery, eliminates disputes over purity, and creates a level playing field for both legitimate and fraudulent vendors. Difficulties: Companies in the newly included zones will incur costs and effort to become registered with BIS, arrange hallmarking through AHCs, and train employees. Costs of compliance: They include registration costs, per-piece hallmarking fees, and logistics costs arising from the distance from AHCs. Business preparedness: Large, well-organized firms are likely to adjust more easily than MSMEs and start-ups. Long-term impact: Over time, mandatory hallmarking is expected to formalise the gold trade further and reduce purity-related complaints, benefiting compliant businesses more than it burdens them. Business Opportunities Created Expanded, standardised market access in districts newly brought under mandatory hallmarking, where compliant sellers gain a competitive edge over non-compliant ones. Consumer confidence-driven sales growth, as buyers increasingly prefer hallmarked jewellery. Opportunities for Assaying and Hallmarking Centres to expand infrastructure in newly covered districts. Demand for compliance consulting is rising as businesses seek expert help to register with the BIS quickly and correctly. Technology and process upgrades, such as better inventory and hallmark-tracking systems. Investment opportunities for organised jewellery retail chains looking to formalise operations in newly regulated markets. Why Choose Corpseed? Navigating a regulatory update like this one figuring out whether your district is newly covered, getting BIS hallmarking registration in place, and making sure every piece of stock is compliant takes time that most business owners don't have. Corpseed works as an end-to-end compliance partner for gold jewellery businesses, handling: BIS hallmarking registration from application to approval Documentation assistance, so your paperwork is accurate the first time Liaison with government and BIS offices on your behalf Application filing for new registrations and renewals Approval tracking, so nothing gets delayed in the pipeline Pan-India support, useful for businesses operating across multiple newly listed districts Dedicated compliance experts who track regulatory updates like this one as they happen. A transparent, step-by-step process with clear timelines Quick turnaround, reducing the time between a new requirement and full compliance Corpseed's Core Message Regulatory updates, such as the Hallmarking of Gold Jewellery and Gold Artefacts (Third Amendment) Order, 2026, move quickly, and non-compliance can lead to penalties, stock issues, and reputational damage. You don't need to track every gazette notification, decode every legal clause, or figure out BIS procedures on your own. Corpseed's regulatory experts monitor these changes as they're published and help businesses move from uncertainty to full compliance without unnecessary delays or risk. If your business deals in gold jewellery or gold artefacts, the smartest move is to confirm your compliance status today, before it becomes a problem tomorrow. Talk to a Corpseed compliance expert now and get clarity on exactly what this order means for your business. Conclusion The Hallmarking of Gold Jewellery and Gold Artefacts (Third Amendment) Order, 2026 has revised the list of areas, on a district-wise basis, where BIS hallmarking is compulsory for gold jewellery and gold artefacts from August 6, 2026 onwards. If your business falls within the newly declared districts, you should confirm that your BIS hallmarking registration is in order and that all your inventory is duly marked. There is no scope for procrastination regarding this obligation, as it is applicable from today onwards. In case there is any doubt in your mind regarding this revision and the process of getting your BIS hallmarking registration and compliance process completed efficiently and effectively, contact the regulatory compliance experts at Corpseed right away for an actionable plan.

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Summary: The Bureau of Indian Standards has established eight Indian Standards covering electrical appliances, network access security, metadata registries, and the C++ programming language. All eight standards were established on 24 July 2026. Four of them replace previous editions that will remain valid concurrently until 24 January 2027. For the other four standards, the notification does not identify a previous Indian Standard for withdrawal. For manufacturers, importers and technology businesses, the notification raises an obvious question: does the establishment of these standards make BIS certification immediately mandatory? The short answer is no-not by this notification alone. Establishing an Indian Standard and making it compulsory are two distinct regulatory actions. A separate Quality Control Order, legislation, government direction, certification condition, tender or contract may be required to make compliance mandatory. Therefore, businesses should not rush into a BIS licence application without first determining: Whether the standard applies to their product or activity, Whether a separate law or Quality Control Order makes it mandatory, Which edition must be followed, Whether testing or certification is required, Whether an existing licence or test report needs updating. This compliance update explains the eight standards, implementation dates, business impact, the BIS certification process, potential costs, and the steps organisations should take before the older editions are withdrawn. Key Highlights of the BIS Notification The most important takeaways are: Eight Indian Standards were established on 24 July 2026. Five standards pertain to the safety of household or commercial electrical appliances. Three standards relate to network security, metadata and software. Four standards replace earlier editions. The four previous editions remain valid until 24 January 2027. Four standards have no predecessor identified for withdrawal. The notification does not, by itself, impose blanket BIS certification. Businesses must separately check QCO, regulatory, contractual and procurement requirements. Companies using an older edition should begin their transition assessment immediately. Particular Details Issuing authority Bureau of Indian Standards Administrative department Department of Consumer Affairs Notification date 27 July 2026 Date of establishment 24 July 2026 Total standards established Eight Electrical-appliance standards Five Information-technology standards Three Standards replacing previous editions Four Standards without a predecessor listed Four Withdrawal date for previous editions 24 January 2027 Legal basis Rule 15 of the Bureau of Indian Standards Rules, 2018 Background of the BIS Standards Framework The Bureau of Indian Standards, or BIS, is India's national standards body, responsible for establishing, revising, amending, and withdrawing Indian Standards for goods, articles, processes, systems, and services. Indian Standards provide common benchmarks for areas such as: Product safety, Performance, Quality, Testing, Marking, Terminology, Interoperability, Information management, Technical procurement. BIS can formulate an Indian Standard domestically or adopt a standard developed by an international organisation. This explains why several standards in the notification reference IEC, ISO, or IEEE publications. Legal Basis of the Notification The notification was issued under Rule 15 of the Bureau of Indian Standards Rules, 2018. Rule 15 empowers BIS to establish Indian Standards and to reaffirm, amend, revise or withdraw them when required. The process normally involves consultation with technical experts, government bodies, industry representatives, laboratories, consumers and other stakeholders. The establishment, revision and withdrawal of Indian Standards are formally notified through the Official Gazette. Which Standards Have Been Established? S. No. Indian Standard Product or subject International reference Status Previous edition Withdrawal date 1 IS 302 (Part 2/Sec 16): 2026 Food waste disposers IEC 60335-2-16: 2022 No predecessor listed NA NA 2 IS 302 (Part 2/Sec 26): 2026 Electrical clocks IEC 60335-2-26: 2024 Second revision IS 302-2-26: 2014 24 January 2027 3 IS 302 (Part 2/Sec 36): 2026 Commercial electric cooking ranges, ovens, hobs and hob elements IEC 60335-2-36: 2021 No predecessor listed NA NA 4 IS 302 (Part 2/Sec 49): 2026 Commercial appliances for keeping food and crockery warm IEC 60335-2-49: 2021 No predecessor listed NA NA 5 IS 302 (Part 2/Sec 54): 2026 Household surface-cleaning appliances using liquids or steam IEC 60335-2-54: 2022 No predecessor listed NA NA 6 IS/ISO/IEC/IEEE 8802-1X: 2021 Port-based network access control ISO/IEC/IEEE 8802-1X First revision 2013 edition 24 January 2027 7 IS/ISO/IEC 11179-6: 2023 Metadata registry registration ISO/IEC 11179-6 First revision 2015 edition 24 January 2027 8 IS/ISO/IEC 14882: 2024 C++ programming language ISO/IEC 14882 Second revision 2020 edition 24 January 2027 Scope of the Notification The standards can be divided into two broad categories. Electrical-Appliance Safety The first five standards form part of the IS 302 series, which covers the safety of household and similar electrical appliances. These standards may be relevant to: Electrical-appliance manufacturers, Commercial-kitchen equipment companies, Domestic appliance brands, Importers, Foreign manufacturers, Distributors, Testing laboratories, Hotels and restaurants, Hospitals and institutional kitchens, Government and private procurement agencies. Information Technology and Software The remaining three standards relate to: Port-based network access control, Metadata registry registration, and The C++ programming language. These standards may be relevant to: Network-equipment manufacturers, Cybersecurity service providers, System integrators, Government IT departments, Data-governance teams, Software companies, Compiler developers, Embedded-system manufacturers, Technology procurement teams. The compliance implications are different for each group. An electrical product may be subject to product testing and certification if covered by a mandatory order. An IT or software standard may instead become relevant through procurement, contracts, technical policies, or voluntary adoption. Detailed Explanation of the Eight Standards 1. IS 302 (Part 2/Sec 16): 2026-Food Waste Disposers This standard is based on IEC 60335-2-16: 2022 and relates to the safety of electrically operated food waste disposers. Food waste disposers are typically installed in kitchen sink systems and are designed to break down food waste before disposal. The Gazette does not list an earlier Indian Standard for withdrawal. Businesses should therefore describe it as a standard for which no predecessor is identified in this notification. It should not be claimed that no other safety requirement was previously relevant to these appliances. Who Should Review This Standard? Food waste disposer manufacturers, Kitchen-appliance brands, Modular-kitchen businesses, Importers and distributors, Hotels and restaurants, Builders and institutional buyers, Product testing laboratories. Manufacturers and importers should first compare the product's intended use, design and electrical specifications with the precise scope of the complete standard. They should then check whether a QCO, certification scheme, tender or customer contract makes conformity compulsory. 2. IS 302 (Part 2/Sec 26): 2026-Electrical Clocks This standard is based on IEC 60335-2-26: 2024 and specifies particular safety requirements for electrical clocks. It is the second revision and replaces IS 302-2-26: 2014. However, the previous edition will remain valid until 24 January 2027. Manufacturers should analyze: Models tested in accordance with the 2014 version, Any BIS license that is in place, as applicable, Test reports, Product drawings, Critical parts, Markings and instructions for users, Applications pending, Specification of suppliers. The notification is not a summary of the technical differences between the 2014 and 2026 versions. The assessment of the transition will require a clause-by-clause comparison of all standards. 3. IS 302 (Part 2/Sec 36): 2026-Commercial Electric Cooking Appliances This standard is based on IEC 60335-2-36: 2021. It covers commercial electric cooking ranges, ovens, hobs and hob elements. The standard may be relevant to equipment used in: Hotels, Restaurants, Canteens, Hospitals, Cloud kitchens, Catering facilities, Institutional kitchens, Food-service businesses. No predecessor Indian Standard is identified for withdrawal in the notification. Commercial appliances can differ from ordinary household appliances in their intended use, operating environment, capacity and frequency of operation. A company should not classify a product solely by the words "oven" or "hob." The complete scope and definitions must be reviewed before beginning the BIS certification process. 4. IS 302 (Part 2/Sec 49): 2026-Appliances for Keeping Food and Crockery Warm This standard is based on IEC 60335-2-49: 2021. It concerns commercial electrical appliances used for keeping food or crockery warm. The standard may be relevant to manufacturers and suppliers serving: Restaurants, Hotels, Buffets, Hospitals, Catering businesses, Commercial cafeterias, Institutional kitchens. No previous Indian Standard is listed for withdrawal. Manufacturers should examine the product's commercial purpose, heating method, electrical characteristics and intended operating conditions before deciding that the standard applies. Institutional purchasers may also begin referring to this standard in procurement documents even where no independent QCO makes it mandatory. 5. IS 302 (Part 2/Sec 54): 2026-Liquid- and Steam-Based Surface Cleaners This standard is based on IEC 60335-2-54: 2022 and covers household surface-cleaning appliances that use liquids or steam. The exact scope must be checked before classifying steam cleaners, liquid-based cleaners, or multipurpose cleaning equipment under this standard. Possible impacted industries: Manufacturers of cleaning appliances, Brands of consumer electronics, Importers, Foreign manufacturers, Distributors, Online retailers, Product-testing labs. Importers need to conduct a BIS applicability study before placing a large purchase order or delivering products to India. Finding out that there is a mandatory compliance requirement after delivery could result in storage costs, delayed launches, and retesting. 6. IS/ISO/IEC/IEEE 8802-1X: 2021-Port-Based Network Access Control This standard concerns port-based network access control for local and metropolitan area networks. It replaces the 2013 edition, which is scheduled for withdrawal on 24 January 2027. Port-based network access control helps organisations manage how devices and users obtain access to network infrastructure. The standard may be relevant to: Network-equipment manufacturers, Enterprise security teams, Cybersecurity companies, System integration firms, Managed services providers, IT Projects by Government, Operators of Critical Infrastructure. Companies relying on the old version must carefully examine contracts, technical designs, procurement requirements, and product documentation. The notification does not require every organisation to redesign its network. Applicability may arise through customer requirements, security policies, contracts or public procurement. 7. IS/ISO/IEC 11179-6: 2023-Metadata Registry Registration This standard deals with the registration of metadata in a metadata registry. It replaces the 2015 edition, which will remain valid until 24 January 2027. Metadata registries help organisations maintain structured information about data elements. They may support: Data governance, Common definitions, Information exchange, Data interoperability, Institutional record management, Standardised data dictionaries. The standard may be relevant to government departments, financial institutions, healthcare organisations, digital platforms and large enterprises. Organisations using the previous edition should review their registration procedures, governance roles, metadata status models, approval mechanisms and related software requirements. 8. IS/ISO/IEC 14882: 2024-C++ Programming Language This standard relates to the C++ programming language and replaces the 2020 edition. The earlier edition will remain valid until 24 January 2027. The standard may be relevant to: Software developers, Compiler vendors, Embedded-system manufacturers, Automotive technology companies, Industrial software companies, Government technology projects, Organisations procuring safety-critical software. Its establishment does not mean that every developer using C++ must obtain BIS registration or certification. Its relevance is more likely to arise through compiler conformity, coding policies, technical contracts, procurement requirements, software development standards, or migration to newer C++ capabilities. What Has Changed? The notification creates three broad changes. Four Standards Have No Predecessor Listed No previous Indian Standard is identified for withdrawal for: Food waste disposers, Commercial electric cooking ranges, ovens and hobs, Commercial food- and crockery-warming appliances, Household liquid- or steam-based surface-cleaning appliances. This does not necessarily mean that these products were completely unregulated earlier. Another general safety standard, QCO certification condition, or sector-specific requirement may still be relevant. Four Standards Replace Previous Editions Older editions have been replaced for: Electrical clocks, Network access control, Metadata registry registration, C++ programming language. These previous editions remain concurrently valid until 24 January 2027. Greater Alignment With International Standards The notification adopts the latest editions of IEC, ISO, and IEEE as Indian Standards. This can help align Indian technical practices with more recent international requirements. However, businesses must use the complete Indian editions when determining domestic compliance. What the Notification Does Not Tell Businesses The Gazette identifies the standards, establishment dates, previous editions, and withdrawal dates. It does not provide: Complete technical requirements, Clause-by-clause changes, Product testing methods, Certification procedures, BIS licence fees, Factory-inspection requirements, Penalties for every affected business, Automatic confirmation that certification is mandatory. These questions require review of the complete standard and the applicable regulatory instrument. Implementation Timeline and Transition Norms Date or period Regulatory position Recommended business action 24 July 2026 All eight Indian Standards established Identify applicable products, systems and contracts 27 July 2026 BIS notification dated Begin legal and technical assessment July 2026 to January 2027 Old and new editions run concurrently for four revised standards Compare editions, update products and complete testing Before 24 January 2027 Transition-planning period Resolve certification, documentation and contractual issues 24 January 2027 Listed previous editions scheduled for withdrawal Move to the new edition, subject to applicable BIS directions After 24 January 2027 Previous editions no longer remain concurrently valid under this notification Maintain conformity with the applicable new edition What Does Concurrent Running Mean? Concurrent running allows two editions of an Indian Standard to remain valid for a specified period. Rule 28 of the Bureau of Indian Standards Rules, 2018 permits the Director General of BIS to allow concurrent operation of two versions and determine the transition period. Businesses should use this period for orderly migration. It should not be treated as a reason to wait until January 2027. What About Products Already in the Market? The notification does not provide a universal answer for products manufactured, tested, certified, or imported under an earlier edition. Businesses must separately check: Applicable BIS implementation guidelines, Existing licence conditions, QCO provisions, Acceptance of old test reports, Treatment of products already manufactured, Pending BIS applications, Existing inventory, Contractual obligations. Why Were These Standards Implemented? The notification does not provide a detailed policy explanation for each standard. However, the updates appear consistent with recognised standardisation objectives. Updating Electrical-Safety Benchmarks Electrical appliances and their components continue to evolve. Updated standards can provide more current benchmarks for design, construction, testing and safe use. Aligning India With International Standards The use of newer IEC, ISO and IEEE editions can reduce differences between Indian and international technical practices. This may help manufacturers operating in multiple markets, although Indian regulatory and certification requirements must still be assessed separately. Improving Network Security The network-access-control standard provides an updated technical reference for controlling access to local and metropolitan networks. Strengthening Data Governance The metadata-registry standard can support consistent data definitions, registration procedures and information exchange. Updating Software Specifications The new C++ edition provides a more up-to-date reference for developers, compiler vendors and organisations that specify C++ requirements in contracts or procurement. Impact on Businesses Impact on Manufacturers Manufacturers may need to review product designs, components, drawings, technical files, quality-control plans, testing capabilities, and existing certifications. Where the new edition contains materially different requirements, the manufacturer may need to: Modify product construction, Replace critical components, Update testing equipment, Conduct additional testing, Revise user instructions, Update product marking, Amend supplier specifications, Extend or change an existing licence. The actual changes cannot be confirmed from the Gazette alone. Impact on Importers Importers should check product compliance before placing orders or arranging shipment. A delayed regulatory assessment may result in: Shipment delays, Additional warehousing costs, Product testing after manufacture, Re-labelling, Supplier disputes, Delayed market launch, Certification expenses not included in the original budget. The manufacturer, rather than the importer, may need to hold the BIS licence under certain product-certification schemes. The correct applicant must be identified before filing. Impact on Foreign Manufacturers BIS certification for foreign manufacturers may involve additional documentation and coordination. Depending on the applicable scheme, the process may require: Appointment of an authorised Indian representative, Overseas-factory information, Product testing, Factory inspection, Travel and inspection expenditure, Brand authorisation, Ongoing representation in India. Foreign manufacturers should begin the process well before the planned Indian launch date. Impact on MSMEs Micro and small businesses may face a proportionately greater burden because they may not have: An in-house compliance department, Complete testing infrastructure, Dedicated regulatory personnel, Experience with BIS applications, Sufficient budget for repeated testing, Easy access to specialised laboratories. An early gap analysis can help an MSME avoid unnecessary product modifications and incorrect applications. Impact on Hotels, Restaurants and Institutional Buyers Hotels, hospitals, restaurants, canteens and commercial kitchens may be affected through procurement. Buyers may begin asking suppliers for: Updated conformity evidence, Valid BIS licences, where applicable, Test reports, Product-safety declarations, Confirmation of the relevant Indian Standard, Technical specifications aligned with the new edition. Impact on Technology Companies Technology businesses may need to review: Network-security architecture, IT procurement documents, Customer contracts, Metadata-governance procedures, Data dictionaries, Compiler support, Coding standards, Toolchain policies, Software migration plans. How Businesses Can Achieve Compliance A business should approach the notification through a structured process. Step 1: Complete an Applicability Assessment The business should begin with the product's: Intended use, Technical design, Electrical rating, User category, Operating environment, Manufacturing process, Commercial description. Similar products may fall under different standards. Choosing a standard based only on a product name can result in an incorrect BIS licence application. Step 2: Verify Mandatory Status Search for: Quality Control Orders, Product-specific BIS certification manuals, Regulatory notifications, Applicable conformity-assessment schemes, Tender requirements, Customer contracts, Sector-specific directions. This is one of the most important functions of a BIS certification consultant. Step 3: Obtain the Complete Standard The Gazette is only a notification. It cannot be used as a replacement for the complete technical standard. The complete standard must be reviewed for: Scope, Definitions, Classifications, Construction requirements, Safety requirements, Test methods, Marking, Documentation, Referenced standards. Step 4: Conduct a Gap Analysis For the updated standards, enterprises need to conduct a clause-by-clause comparison between the old and updated editions. Gap analysis will help determine: New requirements, New tests, New definitions, New classification, New references, Product design considerations, Changes in documentation, Requirement for retesting. Step 5: Prepare Technical Documentation Documents may include: Process chart for manufacturing, Factory layout, List of machinery, Testing equipment list, Calibration certificates, Drawings of products, Bills of material, Component specifications, Ratings of product, Product models, Quality control plan, Test reports, Trademark documents. The final document list depends on the product and BIS scheme. Step 6: Complete Product Testing Where testing is required, the business should verify: Laboratory recognition or acceptance, Testing scope, Sample quantity, Testing duration, Test charges, Report validity, Model-grouping rules, Retesting conditions. Choosing the wrong BIS testing laboratory can lead to an unusable report and repeated expenditure. Step 7: Submit the BIS Licence Application A complete application should correctly identify: Manufacturer, Manufacturing unit, Product category, Indian Standard, Product models, Brand, Applicable certification scheme, Test reports, Authorised representatives. Incomplete or inconsistent information can delay the BIS certification process. Step 8: Prepare for Factory Inspection Where factory inspection is required, the manufacturer should ensure that: Production facilities are operational, Testing equipment is available, Calibration certificates are valid, Quality-control procedures are implemented, Technical personnel are present, Records are properly maintained, Product samples can be drawn. Step 9: Update Product Marking The BIS Standard Mark must only be used under a valid licence and within its approved scope. Product marking may need to include: Licence number, Product identification, Model, Rating, Traceability information, Applicable statutory declarations, User and safety instructions. Step 10: Maintain Post-Certification Compliance BIS compliance continues after the licence is granted. Manufacturers may need to maintain: Routine test records, Calibration, Quality-control records, Supplier controls, Complaint records, Correct use of the Standard Mark, Surveillance readiness, Renewal documents, Change notifications, Compliance with later amendments. BIS Certification Cost There is no single BIS certification cost for every product. The total cost depends on the standard, product, certification scheme, testing requirements, and location of the manufacturing unit. Cost component Main factors affecting cost BIS application fee Certification scheme and number of applications Laboratory testing Product complexity, tests, samples and laboratory charges Inspection expenses Factory location and inspection requirements Foreign-manufacturer expenses Overseas inspection, travel and sample shipment Product redesign Nature and number of technical non-conformities Retesting Test failure, sample modification or additional models Marking fee Product category, production volume and licence conditions Professional charges Scope of BIS certification services required Internal compliance cost Staff, equipment, calibration and training Renewal and surveillance Applicable licence and continuing-compliance requirements Businesses should request a product-specific quotation rather than relying on a generic BIS certification cost displayed online. A basic quotation may not include: Government fees, Laboratory charges, Factory inspection, Travel expenses, Sample shipment, Product redesign, Retesting, Additional model coverage, Marking fees, Post-certification support. Risks of Ignoring the Updated Standards Even where a standard is not independently mandatory, ignoring it may create commercial or contractual risks. These can include: Rejection from government or private tenders, Failure to meet customer specifications, Use of an outdated technical reference, Rejection of test reports, Delayed BIS certification, Repeat testing, Product redesign after launch, Supplier disputes, Loss of customer confidence, Network-security weaknesses, Inconsistent metadata governance, Software compatibility issues. Where a separate QCO makes certification mandatory, non-compliance may also lead to enforcement under the applicable order and the BIS Act. The penalties should be linked to the mandatory instrument, not incorrectly attributed solely to this standards-establishment notification. Benefits for Businesses Improved Product Safety Updated electrical appliance standards can support safer product design, manufacturing, and testing. Greater International Alignment International coordination will help reduce the gap between the technical procedures followed in India and those defined internationally by the latest IEC, ISO, and IEEE standards. Better Market Credibility Conformity with recognised standards can improve confidence among customers, institutional buyers, and business partners. Clearer Procurement Standards make it possible for buyers to quantify specifications of products/systems/suppliers. Reduced Product Failure Risk Effective testing and quality control can reduce defects, complaints, recalls, and corrective action expenses. Stronger Network Security The port-based network access control standard can support more consistent authentication and access management practices. Improved Data Governance The metadata-registry standard can help organisations maintain consistent definitions and registration processes. Updated Software Practices The newer C++ standard provides a current reference for compilers, development policies, contracts and procurement. Is This the Right Decision or an Additional Burden? The notification represents necessary technical modernisation, but it may also create short-term costs. Why the Decision Is Beneficial The updated standards can: Replace outdated technical references, Increase product safety, Align internationally, Improve procurement processes, Ensure consistent testing, Improve network security, Support better data governance, Modernise software specifications. Why Businesses May See It as a Burden Businesses may need to spend money on: Purchasing the new standards, Technical interpretation, Product redesign, Laboratory testing, Retesting, BIS certification, Documentation, Supplier changes, Staff training, Software migration. The burden may be greater for MSMEs, foreign manufacturers, and companies with several products or manufacturing units. Balanced Assessment The new standards will be beneficial, as technical requirements change with evolving products and technologies. However, successful implementation depends on: Clear BIS transition guidelines, Adequate laboratory capacity, Reasonable certification timelines, Support for MSMEs, Transparent cost structures, Clarity on mandatory applicability. The standards themselves are not the main problem. The burden arises when businesses do not know whether a standard is mandatory, which edition applies, or what must be done with existing products and certificates. Business Opportunities Created The notification can create new commercial opportunities across compliance, engineering, and technology services. BIS Certification and Product Compliance Services Manufacturers and importers may need help with: Product classification, Standard selection, QCO applicability, BIS licence applications, Documentation, Testing, Inspection preparation, Post-certification compliance. Testing-Laboratory Services Testing laboratories may see increased demand for product evaluation under the new electrical-appliance standards. Product Redesign and Safety Engineering Manufacturers that are now opting for newer standards may require support with components, construction, technical drawings, and safety assessments. Foreign-Manufacturer Compliance Services International brands entering India may need assistance with BIS certification, local representation, testing, and factory inspections. Cybersecurity Consulting The network-access-control standard may create opportunities for: Network-security consultants, Authentication solution providers, System integrators, Security auditors, Managed service providers. Metadata and Data-Governance Services Organizations could seek help with their metadata registries, data dictionaries, governance procedures, and digital transformation projects. C++ Training and Migrations Software firms might need: Developer training, Compiler migration, Codebase analysis, Toolchain validation, Compatibility testing, Coding policy updates. Compliance Technology Platforms Businesses with several products may invest in software for: Certificate tracking, Regulatory monitoring, Test-report management, Supplier compliance, Product-model mapping, Renewal reminders. How Can Corpseed Help? The most difficult part of a BIS compliance update is not reading the standard's name. It is determining whether that standard applies to a specific product and what the business must do next. Corpseed can support manufacturers, importers, startups, and foreign companies through the following services. Product and Standard Applicability Assessment Corpseed can analyze the product description, specifications, purpose, and manufacturing process to determine which Indian Standard applies. This reduces the risk of choosing the wrong standard or submitting an unnecessary application. QCO and Mandatory-Status Assessment Before beginning certification, Corpseed can help determine whether the standard is: Voluntary, Covered by a QCO, Required by another regulation, Included in a tender, Contractually mandatory. BIS Certification Support Where certification is required, Corpseed can assist with: Document checklists, Application preparation, Online filing coordination, Response to application queries, Inspection preparation, Application tracking, Post-certification requirements. BIS Testing Laboratory Coordination Corpseed can help businesses understand the required tests, sample requirements, and appropriate laboratory route. Final laboratory selection must be based on the relevant standard, testing scope, and applicable BIS requirements. Transition Gap Analysis Businesses using a previous edition can be supported in comparing their existing products, reports, and documentation with the updated standard. This can help create a structured transition plan before 24 January 2027. Support for Foreign Manufacturers and Importers Assistance may include: India-specific regulatory mapping, Identification of applicant, Authorised Indian representative (AIR) requirements, Documentation, Testing coordination, Factory-inspection preparation, Application support. Compliance Documentation Corpseed can help organise: Product documents, Factory details, Testing records, Quality-control procedures, Brand authorisations, Technical declarations, Application forms. Regulatory Monitoring Future amendments, Quality Control Orders and implementation guidelines can change a business's obligations. Ongoing monitoring helps manufacturers and importers act before a deadline disrupts production, imports or sales. Corpseed can support the application and compliance process, but testing outcomes and licence approval remain subject to BIS requirements and the decision of the competent authority.